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Nature Genetics
|
April 1, 1997
Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor
A M Motley, E H Hettema, E M Hogenhout, et al.
Neurology. Clinical Practice
|
December 10, 2020
Mechanisms of calcification in Fahr disease and exposure of potential therapeutic targets
Melissa E M Peters, Esther J M de Brouwer, Jonas W Bartstra, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 7, 2000
Multidrug-resistance protein 5 is a multispecific organic anion transporter able to transport nucleotide analogs
J Wijnholds, C A Mol, L van Deemter, et al.
Neurology
|
May 1, 1993
Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a)
J E Hoogendijk, E A Janssen, A A Gabreëls-Festen, et al.
Atherosclerosis
|
August 23, 2011
Meta-analysis of the association between single nucleotide polymorphisms in TGF-β receptor genes and abdominal aortic aneurysm
Erik Biros, Paul E Norman, Gregory T Jones, et al.
Journal of Bacteriology
|
March 8, 2011
Genome sequence of Neisseria meningitidis serogroup B strain H44/76
J R Piet, R A G Huis in 't Veld, B D C van Schaik, et al.
European Heart Journal Open
|
August 3, 2022
Evaluation of the cardiac amyloidosis clinical pathway implementation: a real-world experience
Maaike Brons, Steven A Muller, Frans H Rutten, et al.
Nature Genetics
|
June 3, 2000
Mutations in ABCC6 cause pseudoxanthoma elasticum
A A Bergen, A S Plomp, E J Schuurman, et al.
The New England Journal of Medicine
|
May 21, 2010
Long-term outcome of open or endovascular repair of abdominal aortic aneurysm
Jorg L De Bruin, Annette F Baas, Jaap Buth, et al.
Bioinformatics (Oxford, England)
|
December 20, 2000
USAGE: a web-based approach towards the analysis of SAGE data. Serial Analysis of Gene Expression
A H van Kampen, B D van Schaik, E Pauws, et al.
Page
of 25
Search research articles
Search
Showing results (161-170 of 245) with videos related to
Sort By:
Page
of 25
Nature Genetics
|
April 1, 1997
Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor
A M Motley, E H Hettema, E M Hogenhout, et al.
Neurology. Clinical Practice
|
December 10, 2020
Mechanisms of calcification in Fahr disease and exposure of potential therapeutic targets
Melissa E M Peters, Esther J M de Brouwer, Jonas W Bartstra, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 7, 2000
Multidrug-resistance protein 5 is a multispecific organic anion transporter able to transport nucleotide analogs
J Wijnholds, C A Mol, L van Deemter, et al.
Neurology
|
May 1, 1993
Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a)
J E Hoogendijk, E A Janssen, A A Gabreëls-Festen, et al.
Atherosclerosis
|
August 23, 2011
Meta-analysis of the association between single nucleotide polymorphisms in TGF-β receptor genes and abdominal aortic aneurysm
Erik Biros, Paul E Norman, Gregory T Jones, et al.
Journal of Bacteriology
|
March 8, 2011
Genome sequence of Neisseria meningitidis serogroup B strain H44/76
J R Piet, R A G Huis in 't Veld, B D C van Schaik, et al.
European Heart Journal Open
|
August 3, 2022
Evaluation of the cardiac amyloidosis clinical pathway implementation: a real-world experience
Maaike Brons, Steven A Muller, Frans H Rutten, et al.
Nature Genetics
|
June 3, 2000
Mutations in ABCC6 cause pseudoxanthoma elasticum
A A Bergen, A S Plomp, E J Schuurman, et al.
The New England Journal of Medicine
|
May 21, 2010
Long-term outcome of open or endovascular repair of abdominal aortic aneurysm
Jorg L De Bruin, Annette F Baas, Jaap Buth, et al.
Bioinformatics (Oxford, England)
|
December 20, 2000
USAGE: a web-based approach towards the analysis of SAGE data. Serial Analysis of Gene Expression
A H van Kampen, B D van Schaik, E Pauws, et al.
Page
of 25